GPR99, a new G protein-coupled receptor with homology to a new subgroup of nucleotide receptors
- Timo Wittenberger†1,
- Susanne Hellebrand†1,
- Antonia Munck1,
- Hans-Jürgen Kreienkamp2,
- H Chica Schaller1 and
- Wolfgang Hampe1Email author
© Wittenberger et al; licensee BioMed Central Ltd. 2002
Received: 12 March 2002
Accepted: 5 July 2002
Published: 5 July 2002
Based on sequence similarity, the superfamily of G protein-coupled receptors (GPRs) can be subdivided into several subfamilies, the members of which often share similar ligands. The sequence data provided by the human genome project allows us to identify new GPRs by in silico homology screening, and to predict their ligands.
By searching the human genomic database with known nucleotide receptors we discovered the gene for GPR99, a new orphan GPR. The mRNA of GPR99 was found in kidney and placenta. Phylogenetic analysis groups GPR99 into the P2Y subfamily of GPRs. Based on the phylogenetic tree we propose a new classification of P2Y nucleotide receptors into two subgroups predicting a nucleotide ligand for GPR99. By assaying known nucleotide ligands on heterologously expressed GPR99, we could not identify specifically activating substances, indicating that either they are not agonists of GPR99 or that GPR99 was not expressed at the cell surface. Analysis of the chromosomal localization of all genes of the P2Y subfamily revealed that all members of subgroup "a" are encoded by less than 370 kb on chromosome 3q24, and that the genes of subgroup "b" are clustered on one hand to chromosome 11q13.5 and on the other on chromosome 3q24-25.1 close to the subgroup "a" position. Therefore, the P2Y subfamily is a striking example for local gene amplification.
We identified a new orphan receptor, GPR99, with homology to the family of G protein-coupled nucleotide receptors. Phylogenetic analysis separates this family into different subgroups predicting a nucleotide ligand for GPR99.
The superfamily of G protein-coupled receptors (GPRs) is one of the largest human gene families . Many different approaches have been undertaken to identify new GPRs, both biochemically and by database searches. Recently, we have identified several new GPR genes from the database of expressed sequence tags by a complex computational strategy . With the availability of the human genomic sequence another source for data mining became accessible, which is especially valuable for GPR searches, since many GPR genes contain no or only a few introns. Nevertheless, the existance of pseudogenes, many of which are not transcribed or lead to truncated proteins, makes it necessary to prove the expression of each putative gene found in the genome. For this publication we used some of the new receptors with homology to the subfamily of P2Y nucleotide receptors  to search for further GPRs in the human genomic database.
Results and discussion
Identification of GPR99
A closer analysis of residues implicated in direct nucleotide interactions confirms the existance of two distinct nucleotide receptor subgroups. At the beginning of transmembrane domain seven, all receptors of subgroup "b", including GPR99, share the motif Y-X-V-T-R-P-L, which is not found in the other GPRs (Fig. 3B). The highly specific positively charged arginine residue of this motif was shown to play an important role for binding of negatively charged nucleotides . In the same position the subgroup "a" members share the motif K-E-X-T-L-X-L. P2Y5, P2Y7, P2Y9, P2Y10 and other non-nucleotide receptors lack both of these motifs (Fig. 3B). These motifs might, therefore, be good diagnostic tools to predict ligands for additional orphan receptors.
Towards the end of transmembrane domain seven many GPRs share the motif D/N-P-X-X-Y. GPR99 lacks the highly conserved proline residue of this motif (Fig. 3B) and shares a leucine residue at this position with two GPRs encoded by Herpes simplex virus six. Since also some melatonin receptors, some retinal receptors, the muscarinic acetylcholine receptor from drosophila, and the orphan receptors GPR35 and GPR52 lack the proline residue at this position, GPR99 might very well be a functional receptor.
All nucleotide-binding GPRs including GPR99 contain the motif H-X-X-R/K at the end of transmembrane domain six, which is shared by only a few other GPRs, like the orphan receptors GPR17 and GPR34.
The BAC clone AC026756.15 contains the GPR99 gene and is part of the contig NT_009840 which maps to chromosome 13q32-33. The Ensembl contig view tool , which identified the GPR99 ORF by automated gene prediction (volatile ID 426046), maps GPR99 to chromosome 13q32.2. To the same chromosomal location two disorders, congenital Microcoria and one form of Schizophrenia, had been linked.
In contrast to other nucleotide GPR genes, which are often found in clusters, we did not recognize further GPR genes close to GPR99. The chromosomal localization of the other nucleotide GPRs supports the proposed subgroup classification, since all genes of the subgroup "a" receptors are located within 355 kb on two overlapping BAC clones (AC024886 and AC078816) on chromosome 3q24 (Fig. 3C). The five subgroup "a" genes are, therefore, excellent examples for gene duplication events and divergent evolution of the resulting genes. The subgroup "b" genes are more scattered throughout the genome with clusters of P2Y1 and GPR91 on chromosome 3q24-25.1, not far away from the subgroup "a" cluster, and of P2Y2 and P2Y6 on chromosome 11q13.5  on the same BAC clone consisting of 191 kb (AP002761).
A full-length cDNA clone of GPR99 was constructed by ligating error-free PCR products. For expression in Xenopus oocytes this cDNA was cloned into pGemHE . In vitro transcribed cRNA was injected together with the cRNA of a G-protein coupled inwardly rectifying potassium channel, and the oocytes were analyzed by whole cell clamp as described [11, 12]. None of the applied nucleotide ligands (ATP, CTP, GTP, UTP, ADP, GDP, UDP, AMP, CMP, GMP, cAMP, cGMP, CMP-sialic acid, GDP-fucose, GDP-mannose, UDP-N-acetyl galactosamin, UDP-glucuronate, UDP-galactose, UDP-N-acetyl glucose) evoked stronger responses in GPR99-injected than in control oocytes. As an additional mammalian expression system we used CHO cells stably transfected with aequorin and the promiscous G protein α subunit Gα16. These cells were transiently transfected with a GPR99-pcDNA3 construct. G-protein activation was analyzed by measuring the Ca2+-dependent luminescence of aequorin in a bioluminometer (Berthold). As in the oocyte system, the above mentioned nucleotides did not stimulate the emission of light in a GPR99-dependent manner. We conclude from this that the nucleotide derivatives assayed are either no agonists of GPR99 or that GPR99 can not activate the G proteins present in the oocyte and the CHO cells. Both systems are widely used for heterologous cell-surface expression of GPRs. Nevertheless, since no GPR99-specific antiserum was available, and since we did not add an epitope tag to GPR99, we can not prove cell-surface expression which is a prerequisite for the ligand assays used.
We describe the identification of GPR99 from human genomic data and its expression in kidney and placenta. With respect to a new subgroup classification for the P2Y subfamily based on sequence similarity, specific ligand-binding motifs, and gene clustering, we propose that GPR99 is a receptor for nucleotide ligands.
Materials and methods
Database searches and construction of evolutionary trees
BLASTN and TBLASTN searches of GenBank were performed using the National Center for Biotechnology Information server . Amino-acid sequences were aligned with Clustal W . Phylogenetic analysis was performed using the program PUZZLE , a support value of at least 53% was assigned to each internal branch.
A commercial human multiple-tissue northern blot (Clontech) was hybridized using a [32P]-labeled 400 bp NotI-GPR99 fragment of the IMAGE clone 3014233 (AW827323) according to the manufacturer's instructions. The blot contained 1 μg of poly-A+ RNA in each lane.
Based on the genomic sequence of hGPR99 an upstream primer containing the in-frame stop and start codon (AGA TGA AAG GAG ACA ACC ATG AAT G) and a downstream primer about 50 nucleotides 3' of the stop codon (CTT AGG ATG CTA GGT AAA GTA TCA GC) were designed. Full-length GPR99 was PCR amplified from placental cDNA prepared with the Marathon kit (Clontech) using a protocol with 30 cycles at an annealing temperature of 55°C and Taq polymerase.
To obtain an error-free GPR99 cDNA, the PCR products were cloned into the pGEM-T Easy vector (Promega) and a full-length clone was constructed by ligating error-free parts of two individual clones.
For expression in Xenopus oocytes GPR99 was cloned into pGemHE . In vitro transcribed cRNA was injected together with the cRNA of the G protein-coupled inwardly-rectifying potassium channel GIRK, and the oocytes were analyzed by whole cell clamp analysis [11, 12].
As a mammalian expression system we used CHO cells stably transfected with aequorin and the promiscuous G protein α subunit Gα16. These cells were transiently transfected with GPR99 cloned into pcDNA3 (Invitrogen). Activation of G-proteins was analyzed by measuring the Ca2+-dependent luminescence of aequorin in a bioluminometer (Berthold).
T. W. and S. H. caried out the phylogenetic and sequence analysis, A. M. performed the aequorin assay, and H.-J. K. the Xenopus oocyte assay. H.C.S. participated in the design of the study and W. H. initially identified and sequenced gpr99, took part in the ligand assays, and wrote the manuscript. All authors read and approved the final manuscript.
We thank P. Joost and A. Methner for discussions and S. Hempel for help with the figures. This work was supported by the Deutsche Forschungsgemeinschaft (SFB 444 and 545).
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